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Journal ArticleDOI

Chemical characterization of silicon-substituted hydroxyapatite.

TLDR
Chemical analysis confirmed the proposed substitution of the silicon (or silicate) ion for the phosphorus (or phosphate) ion in hydroxyapatite and demonstrated that phase-pure silicon-substituted hydroxyAPatite may be prepared using a simple precipitation technique.
Abstract
Bioceramic specimens have been prepared by incorporating a small amount of silicon (0.4 wt %) into the structure of hydroxyapatite [Ca10(PO4)6(OH)2, HA] via an aqueous precipitation reaction to produce a silicon-substituted hydroxyapatite (Si-HA). The results of chemical analysis confirmed the proposed substitution of the silicon (or silicate) ion for the phosphorus (or phosphate) ion in hydroxyapatite. The Si-HA was produced by first preparing a silicon-substituted apatite (Si-Ap) by a precipitation process. A single-phase Si-HA was obtained by heating/calcining the as-prepared Si-Ap to temperatures above 700 degrees C; no secondary phases, such as tricalcium phosphate (TCP), tetracalcium phosphate (TeCP), or calcium oxide (CaO), were observed by X-ray diffraction analysis. Although the X-ray diffraction patterns of Si-HA and stoichiometric HA appeared to be identical, refinement of the diffraction data revealed some small structural differences between the two materials. The silicon substitution in the HA lattice resulted in a small decrease in the a axis and an increase in the c axis of the unit cell. This substitution also caused a decrease in the number of hydroxyl (OH) groups in the unit cell, which was expected from the proposed substitution mechanism. The incorporation of silicon in the HA lattice resulted in an increase in the distortion of the PO4 tetrahedra, indicated by an increase in the distortion index. Analysis of the Si-HA by Fourier transform infrared (FTIR) spectroscopy indicated that although the amount of silicon incorporated into the HA lattice was small, silicon substitution appeared to affect the FTIR spectra of HA, in particular the P-O vibrational bands. The results demonstrate that phase-pure silicon-substituted hydroxyapatite may be prepared using a simple precipitation technique.

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Citations
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Journal ArticleDOI

Preparation of Silicate Substituted Calcium Deficient Hydroxyapatite by Coprecipitation

TL;DR: In this paper, a typical coprecipitation method to synthesize silicate-substituted calcium deficient hydroxyapatite (SiCDHA) was presented, and the results showed that the so-prepared samples were SiCDHA.
Book ChapterDOI

Role of substitution in bioceramics

TL;DR: Apatite is the major constituent and mineral phase of bone, dentin, and enamel as mentioned in this paper, which allows substitution, doping, and grafting of different ions, small functional compounds, peptides, and polymers.
Journal ArticleDOI

Reaction-bonded bioresorbable composite material

TL;DR: A series of composite materials based on dicalcium phosphate dihydrate and bioactive glass 50S25N5P with physiologically safe pH and compression strength from 4 to 22 MPa has been developed as mentioned in this paper.
Book ChapterDOI

Bone Substitute Materials

Marc Bohner
TL;DR: In this article, the main resorption mechanisms of bone substitute materials are discussed, with an emphasis on four aspects: (1) the various materials used for bone substitution, (2) various formulations that are commercially available (granules, blocks, pastes, cements, membranes), (3) the special architectures used for such materials, and finally (4) the main reorption mechanism of bone substitutes.
Journal ArticleDOI

Functional role of inorganic trace elements in dentin apatite-Part II: Copper, manganese, silicon, and lithium.

TL;DR: In this article , the functional role of copper, manganese, silicon, and lithium on dentin apatite, with critical effects on morphology, crystallinity, and solubility, was evaluated.
References
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Journal ArticleDOI

Bioceramics: From Concept to Clinic

TL;DR: The mechanisms of tissue bonding to bioactive ceramics are beginning to be understood, which can result in the molecular design of bioceramics for interfacial bonding with hard and soft tissues.
Journal Article

Bioceramics : from concept to clinic

TL;DR: The mechanisms of tissue bonding to bioactive ceramics are beginning to be understood, which can result in the molecular design of bioceramics for interfacial bonding with hard and soft tissues.
Journal ArticleDOI

Silicon: A Possible Factor in Bone Calcification

TL;DR: Silicon, a relatively unknown trace element in nutritional research, has been uniquely localized in active calcification sites in young bone and is suggested to be associated with calcium in an early stage of calcification.
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